The trapping of a phosphinidene (R-P) in an NCN pincer is presented. Stabilized phosphinidene 1 was characterized by P{ H}, H, and C{ H} NMR spectroscopy, exhibiting an averaged C symmetry in solution between -60 and 60 °C. In the solid state, the phosphinidene is coordinated by one adjacent N atom featuring a formal P-N bond (1.757(2) Å) to give a five-membered ring with some aromatic character, confirmed by DFT calculations (B3LYP-D3/6-311G**++) to be the ground-state structure. Equilibration of the two N ligands occurs rapidly in solution via a "bell-clapper"-type process through an associative symmetric transition state calculated to lie 4.0 kcal mol above the ground state.
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http://dx.doi.org/10.1002/chem.201604415 | DOI Listing |
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